Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:1685129rdf:typepubmed:Citationlld:pubmed
pubmed-article:1685129lifeskim:mentionsumls-concept:C0011849lld:lifeskim
pubmed-article:1685129lifeskim:mentionsumls-concept:C0332307lld:lifeskim
pubmed-article:1685129lifeskim:mentionsumls-concept:C1708726lld:lifeskim
pubmed-article:1685129lifeskim:mentionsumls-concept:C1420172lld:lifeskim
pubmed-article:1685129lifeskim:mentionsumls-concept:C0796344lld:lifeskim
pubmed-article:1685129lifeskim:mentionsumls-concept:C0035268lld:lifeskim
pubmed-article:1685129lifeskim:mentionsumls-concept:C0439064lld:lifeskim
pubmed-article:1685129lifeskim:mentionsumls-concept:C0018591lld:lifeskim
pubmed-article:1685129pubmed:issue11lld:pubmed
pubmed-article:1685129pubmed:dateCreated1992-2-24lld:pubmed
pubmed-article:1685129pubmed:abstractTextThe liver/islet glucose transporter (GLUT2) is expressed in the liver and in the Beta cells of pancreatic islets and is a candidate gene for the inherited defect in Type 2 (non-insulin-dependent) diabetes mellitus. A series of restriction fragment length polymorphisms have been identified using a GLUT2 cDNA probe with five restriction enzymes in a British white Caucasian population. Five independent restriction fragment length polymorphisms detected by restriction enzymes EcoRI (two restriction fragment length polymorphisms termed EcoRI-1, EcoRI-2), TaqI (two restriction fragment length polymorphisms termed TaqI-1, TaqI-2), and BclI (BclI-2) were used to construct GLUT2 haplotypes. Significant linkage disequilibrium was observed between four polymorphic sites EcoRI-2, TaqI-1, TaqI-2 and BclI-2 but linkage disequilibrium was not observed with EcoRI-1 polymorphic site and the other four sites. The frequencies of GLUT2 restriction fragment length polymorphisms and haplotypes in 50 Type 2 diabetic subjects and 50 non-diabetic control subjects show no significant differences suggesting that it is unlikely that there is a single major defect of this gene contributing to the inherited susceptibility to Type 2 diabetes in a Caucasian population.lld:pubmed
pubmed-article:1685129pubmed:languageenglld:pubmed
pubmed-article:1685129pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1685129pubmed:citationSubsetIMlld:pubmed
pubmed-article:1685129pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1685129pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1685129pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1685129pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1685129pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1685129pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1685129pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:1685129pubmed:statusMEDLINElld:pubmed
pubmed-article:1685129pubmed:monthNovlld:pubmed
pubmed-article:1685129pubmed:issn0012-186Xlld:pubmed
pubmed-article:1685129pubmed:authorpubmed-author:PaterJJlld:pubmed
pubmed-article:1685129pubmed:authorpubmed-author:WainscoatJ...lld:pubmed
pubmed-article:1685129pubmed:authorpubmed-author:COLEL JLJlld:pubmed
pubmed-article:1685129pubmed:authorpubmed-author:TurnerR CRClld:pubmed
pubmed-article:1685129pubmed:authorpubmed-author:CookJ TJTlld:pubmed
pubmed-article:1685129pubmed:issnTypePrintlld:pubmed
pubmed-article:1685129pubmed:volume34lld:pubmed
pubmed-article:1685129pubmed:ownerNLMlld:pubmed
pubmed-article:1685129pubmed:authorsCompleteYlld:pubmed
pubmed-article:1685129pubmed:pagination817-21lld:pubmed
pubmed-article:1685129pubmed:dateRevised2010-11-18lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:meshHeadingpubmed-meshheading:1685129-...lld:pubmed
pubmed-article:1685129pubmed:year1991lld:pubmed
pubmed-article:1685129pubmed:articleTitleMultiple restriction fragment length polymorphisms at the GLUT2 locus: GLUT2 haplotypes for genetic analysis of type 2 (non-insulin-dependent) diabetes mellitus.lld:pubmed
pubmed-article:1685129pubmed:affiliationNuffield Department of Clinical Medicine, Radcliffe Infirmary, Headington, Oxford, UK.lld:pubmed
pubmed-article:1685129pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1685129pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:1685129lld:pubmed